In addition, this work develops a promising cluster-based aluminum material as iodine adsorbents.As reported herein, the waterborne polymers poly(glycidyl methacrylate-co-poly(ethylene glycol) methyl ether methacrylate) P(GMA-co-mPEGMA) and polyethyleneimine (PEI) were used to prepare multipurpose polyvinylidene fluoride (PVDF) membranes via a direct spray-coating method. P(GMA-co-mPEGMA) and PEI were alternately sprayed onto the PVDF membrane to yield stable cross-linked copolymer coatings. The successful coating of polymers onto the membrane surface was verified by scanning electron microscopy, attenuated total reflectance-Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy characterization. The coated membrane exhibited oil rejection rates that exceeded 99.0% for oil water mixture separation and 98.0% for oil/water emulsion separation. The flux recovery ratio reached 96.7% after bovine serum albumin filtration and washing with water. The removal efficiencies of the coated membrane M3 for Congo red, methyl orange, methylene blue, and crystal violet, Pb(II), Cu(II), and Cd(II) were 82.4, 83.9, 6.3, 26.8, 90.6, 91.3, and 86.2%, respectively. Thus, it can be used for the removal of dyes and heavy metal ions from wastewater. The antibacterial activities of the coated membranes were also confirmed by the inhibition zone tests and confocal laser scanning microscopy analysis. In addition, the cross-linking strategy provides the coated membranes with excellent durability and repeatability. More importantly, the use of water as the solvent can ensure that the application of these membrane coatings proceeds via a very safe and environmentally friendly coating process.Bimetallic transition-metal phosphides are gradually evolving as efficient hydrogen evolution catalysts. In this study, graphene-coated MoP and bimetallic phosphide (MoNiP) nanoparticles (MoP/MoNiP@C) were synthesized via one-step straightforward high-temperature calcination and phosphating process. The precursor was obtained from polyaniline, Ni2+ ions, and phosphomolybdic acid hydrate (PMo12) by solvent evaporation. As expected, MoP/MoNiP@C manifests excellent hydrogen evolution activity with a low overpotential of 134 mV at 10 mA cm-2 and a small Tafel slope of 66 mV dec-1. Furthermore, MoP/MoNiP@C exhibits satisfactory stability for 24 h in the acid electrolyte. The outstanding catalytic performance can be attributed to the synergistic effect of MoP and MoNiP nanoparticles, the graphene coating protecting MoP and MoNiP from corrosion, as well as an increase in the number of active sites because of porous structures. This work can provide the experimental foundation for the simple synthesis of bimetallic phosphates with remarkable hydrogen evolution performance.The magnetic properties and ozone (O3) gas-sensing activity of zinc ferrite (ZnFe2O4) nanoparticles (NPs) were discussed by the combination of the results acquired by experimental procedures and density functional theory simulations. The ZnFe2O4 NPs were synthesized via the microwave-assisted hydrothermal method by varying the reaction time in order to obtain ZnFe2O4 NPs with different exposed surfaces and evaluate the influence on its properties. Regardless of the reaction time employed in the synthesis, the zero-field-cooled and field-cooled magnetization measurements showed superparamagnetic ZnFe2O4 NPs with an average blocking temperature of 12 K. The (100), (110), (111), and (311) surfaces were computationally modeled, displaying the different undercoordinated surfaces. The good sensing activity of ZnFe2O4 NPs was discussed in relation to the presence of the (110) surface, which exhibited low (-0.69 eV) adsorption enthalpy, promoting reversibility and preventing the saturation of the sensor surface. Finally, the O3 gas-sensing mechanism could be explained based on the conduction changes of the ZnFe2O4 surface and the increase in the height of the electron-depletion layer upon exposure toward the target gas. The results obtained allowed us to propose a mechanism for understanding the relationship between the morphological changes and the magnetic and O3 gas-sensing properties of ZnFe2O4 NPs.Glass ceramics composed of Na2O-BaO-Bi2O3-Nb2O5-Al2O3-SiO2 (NBBN-AS) were modified by rare-earth doping and prepared via the melt-quenching process accompanied by controlled crystallization. High-resolution transmission electron microscopy displayed the glassy matrix closely encompassing the nanosized NaNbO3, Ba2NaNb5O15, BaAl2Si2O8, and AlNbO4 crystalline grains. With rare-earth doping, the NBBN-AS glass ceramics' theoretical energy storage density can reach 22.48 J/cm3. This excellent energy storage property is credited with increasing breakdown strength, and numerical simulation was applied to reveal the intrinsic mechanism for increased breakdown strength by rare-earth doping. The charge-discharge results indicated a giant power density of 220 MW/cm3 as well as an ultrafast discharge speed of 11 ns. The results indicate that the glass ceramic can be used in advanced capacitor applications.New kinds of diradical rare-earth metal complexes supported by diazabutadiene (DAD) ligands, [(DAD)2LnN(TMS)2] (1; Ln = Dy, Lu; TMS = SiMe3), were synthesized and studied. https://www.selleckchem.com/products/Vorinostat-saha.html They showed a new [radical-Ln-radical] alignment with distorted square-pyramidal geometry. Structural and density functional theory analysis illustrated the radical anionic nature of the ligands. Magnetic studies revealed antiferromagnetic coupling of the two radicals in 1-Lu. 1-Dy showed typical single-molecule-magnet (SMM) behavior with an effective energy barrier of 231 K, which is much higher than those of similar radical-containing SMMs. Magnetostructural analysis suggests that the anionic [N(TMS)2]- group plays a vital role in the SMM property. This study provides a new platform for further improving the performance of radical-Ln SMMs.ConspectusBecause chemical reactions on/in cosmic ice dust grains covered by amorphous solid water (ASW) play important roles in generating a variety of molecules, many experimental and theoretical studies have focused on the chemical processes occurring on the ASW surface. In laboratory experiments, conventional spectroscopic and mass-spectrometric detection of stable products is generally employed to deduce reaction channels and mechanisms. However, despite their importance, the details of chemical reactions involving reactive species (i.e., free radicals) have not been clarified because of the absence of experimental methods for in situ detection of radicals. Because OH radicals can be easily produced in interstellar conditions by not only the photolysis and/or ion bombardments of H2O but also the reaction of H and O atoms, they are thought to be one of the most abundant radicals on ice dust. In this context, the development of a close monitoring method of OH radicals on the ASW surface may help to elucidate the chemical reactions occurring on the ASW surface.